Table 2.

Single-marker analysis


Locus and genotype

Low grade, range, %

High grade, range, %

All, range, %

Controls, range, %

E I, range, %

E II-IV, range, %
IL-1β -31       
   C/C   8-13.1   10-12.1   18-12.5   45-13.1   11-10.2   7-20.6  
   C/T   30-49.2   35-42.2   65-45.1   146-42.4   52-48.2   13-38.2  
   T/T   23-37.7   38-45.8   61-42.4   153-44.8   45-41.7   14-41.2  
IL-1β + 3954       
   C/C   4-6.7   3-3.7   7-5.0   24-7.2   3-2.8   3-9.4  
   C/T   20-33.3   26-32.1   46-32.6   121-36.3   37-34.6   9-28.1  
   T/T   36-60.0   52-64.2   88-62.4   188-56.5   67-62.6   20-62.5  
IL-1RN 86VNTR       
   1/1   30-46.9   46-52.9   76-50.3   185-53.8   58-51.3   17-47.2  
   1/2   27-42.2   31-35.6   58-38.4   118-34.3   43-38.1   14-38.9  
   1/3   2-3.1   4-4.6   6-4.0   11-3.2   5-4.4   1-2.8  
   2/2   4-6.3   5-5.8   9-6.0   27-7.9   6-5.3   3-8.3  
   2/3
 
1-1.6
 
1-1.1
 
2-1.3
 
2-0.6
 
1-0.9
 
1-2.8
 

Locus and genotype

Low grade, range, %

High grade, range, %

All, range, %

Controls, range, %

E I, range, %

E II-IV, range, %
IL-1β -31       
   C/C   8-13.1   10-12.1   18-12.5   45-13.1   11-10.2   7-20.6  
   C/T   30-49.2   35-42.2   65-45.1   146-42.4   52-48.2   13-38.2  
   T/T   23-37.7   38-45.8   61-42.4   153-44.8   45-41.7   14-41.2  
IL-1β + 3954       
   C/C   4-6.7   3-3.7   7-5.0   24-7.2   3-2.8   3-9.4  
   C/T   20-33.3   26-32.1   46-32.6   121-36.3   37-34.6   9-28.1  
   T/T   36-60.0   52-64.2   88-62.4   188-56.5   67-62.6   20-62.5  
IL-1RN 86VNTR       
   1/1   30-46.9   46-52.9   76-50.3   185-53.8   58-51.3   17-47.2  
   1/2   27-42.2   31-35.6   58-38.4   118-34.3   43-38.1   14-38.9  
   1/3   2-3.1   4-4.6   6-4.0   11-3.2   5-4.4   1-2.8  
   2/2   4-6.3   5-5.8   9-6.0   27-7.9   6-5.3   3-8.3  
   2/3
 
1-1.6
 
1-1.1
 
2-1.3
 
2-0.6
 
1-0.9
 
1-2.8
 

Single-marker analysis of the proinflammatory haplotype IL-1β -31/IL-1 RN 86 VNTR. SNPs at IL-1β -31 and + 3954 were genotyped by allelic discrimination (TaqMan technology, ABI 7700, Aplera, Foster City, CA). IL-1RN 86 VNTR was genotyped by Southern blot after amplification. Alleles were sized relative to a 100-bp ladder (allele 1 = 4 repeats, allele 2 = 2 repeats, allele 3 = 5 repeats, allele 4 = 3 repeats, allele 5 = 6 repeats). Haplotype case-control analysis was performed using HAPMAX. Hardy-Weinberg equilibrium was confirmed for all polymorphisms tested in gastric lymphoma group and controls. Three types of analysis were performed: (1) all patients with primary gastric B-cell lymphoma were compared against controls, (2) patients separated in low-grade and high-grade lymphoma were compared against controls, and (3) patients with disease stage E I were compared against patients with disease stages E II to E IV. Statistical analysis was performed using SISA Binominal program (Uitenbroek, Daan G, Binomial, SISA, http://home.clara.net/sisa/binomial.htm).

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